FDA 510(k), K141371, SONICISION CORDLESS ULTRASONIC DISSECTOR

FDA 510(k), K141371, SONICISION CORDLESS ULTRASONIC DISSECTOR

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510(K) Number: K141371
Device Name: SONICISION CORDLESS ULTRASONIC DISSECTOR
Manufacturer:
Device Classification Name: Instrument, Ultrasonic Surgical
Regulation Number:
Classification Product Code: LFL
Date Received: 05/27/2014
Decision Date: 08/07/2014
Regulation Medical Specialty:
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